Dataset Open Access

HADDOCK screening against human Angiotensin Converting Enzyme 2 (ACE2)

P. I. Koukos; M. Réau; A. M. J. J. Bonvin

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  "publisher": "Zenodo", 
  "DOI": "10.5281/zenodo.3929463", 
  "language": "eng", 
  "title": "HADDOCK screening against human Angiotensin Converting Enzyme 2 (ACE2)", 
  "issued": {
    "date-parts": [
  "abstract": "<p>The novel coronavirus (SARS-CoV-2) that has emerged from Wuhan, China in December 2019 has spread to almost all countries in the world causing a dramatic number of deaths. The current absence of antiviral treatment against the SARS-CoV-2 urges the scientific community to accelerate the drug discovery research process.</p>\n\n<p>One way to identify potential treatments and to be able to administer it swiftly is to focus on drug repurposing studies, i.e. to investigate the SARS-CoV-2 antiviral potential of drugs that have already been approved for human use.</p>\n\n<p>Proteins that are crucial for the survival and replication of the virus are the most attractive targets for such studies. Here we have focused on the Angiotensin Converting Enzyme 2 receptor (ACE2) that acts as one of the main gateways for viral entry in the host cell. We have screened ~2000 compounds against the inhibitor-bound closed form of the receptor.</p>\n\n<p>This is one part of a multi-target screen emphasising the main protease (Mrpo), the RNA-dependent-RNA-polymerase (RdRp) and human ACE2. The other datasets can found at the following locations:</p>\n\n<ul>\n\t<li><a href=\"\">Mpro: Shape-based assay</a></li>\n\t<li><a href=\"\">Mpro: Pharmacophore-based assay</a></li>\n\t<li><a href=\"\">RdRp</a></li>\n</ul>\n\n<p>More information about this screen along with interactive visualisations of the top compounds can be found on our website <a href=\"\"></a>.</p>", 
  "author": [
      "family": "P. I. Koukos"
      "family": "M. R\u00e9au"
      "family": "A. M. J. J. Bonvin"
  "version": "1.0.0", 
  "type": "dataset", 
  "id": "3929463"
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